Name: rs1159327463
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1159327463

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:78030500-78030521 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₉ / dup(T)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₂=0.0000 (0/9130, ALFA)
del(T)₁₁=0.0000 (0/9130, ALFA)
del(T)₁₀=0.0000 (0/9130, ALFA) (+ 12 more)
del(T)₉=0.0000 (0/9130, ALFA)
del(T)₈=0.0000 (0/9130, ALFA)
del(T)₇=0.0000 (0/9130, ALFA)
del(T)₆=0.0000 (0/9130, ALFA)
del(T)₅=0.0000 (0/9130, ALFA)
del(T)₄=0.0000 (0/9130, ALFA)
delTTT=0.0000 (0/9130, ALFA)
delTT=0.0000 (0/9130, ALFA)
delT=0.0000 (0/9130, ALFA)
dupT=0.0000 (0/9130, ALFA)
dupTT=0.0000 (0/9130, ALFA)
dupTTT=0.0000 (0/9130, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: POLR3A : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	9130	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	5856	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2250	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	90	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2160	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	48	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	108	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	440	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	362	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9130	(T)₂₂=1.0000	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	5856	(T)₂₂=1.0000	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	2250	(T)₂₂=1.0000	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	440	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	362	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	108	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	64	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.78030510_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030511_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030512_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030513_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030514_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030515_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030516_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030517_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030518_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030519_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030520_78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030521del
GRCh38.p14 chr 10	NC_000010.11:g.78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030520_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030519_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030518_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030517_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030516_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030513_78030521dup
GRCh38.p14 chr 10	NC_000010.11:g.78030510_78030521dup
GRCh37.p13 chr 10	NC_000010.10:g.79790268_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790269_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790270_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790271_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790272_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790273_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790274_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790275_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790276_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790277_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790278_79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790279del
GRCh37.p13 chr 10	NC_000010.10:g.79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790278_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790277_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790276_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790275_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790274_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790271_79790279dup
GRCh37.p13 chr 10	NC_000010.10:g.79790268_79790279dup
POLR3A RefSeqGene	NG_029648.1:g.4030_4041del
POLR3A RefSeqGene	NG_029648.1:g.4031_4041del
POLR3A RefSeqGene	NG_029648.1:g.4032_4041del
POLR3A RefSeqGene	NG_029648.1:g.4033_4041del
POLR3A RefSeqGene	NG_029648.1:g.4034_4041del
POLR3A RefSeqGene	NG_029648.1:g.4035_4041del
POLR3A RefSeqGene	NG_029648.1:g.4036_4041del
POLR3A RefSeqGene	NG_029648.1:g.4037_4041del
POLR3A RefSeqGene	NG_029648.1:g.4038_4041del
POLR3A RefSeqGene	NG_029648.1:g.4039_4041del
POLR3A RefSeqGene	NG_029648.1:g.4040_4041del
POLR3A RefSeqGene	NG_029648.1:g.4041del
POLR3A RefSeqGene	NG_029648.1:g.4041dup
POLR3A RefSeqGene	NG_029648.1:g.4040_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4039_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4038_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4037_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4036_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4033_4041dup
POLR3A RefSeqGene	NG_029648.1:g.4030_4041dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1751_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1752_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1753_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1754_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1755_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1756_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1757_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1758_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1759_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1760_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1761_1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1762del
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1761_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1760_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1759_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1758_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1757_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1754_1762dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1751_1762dup

Gene: POLR3A, RNA polymerase III subunit A (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
POLR3A transcript	NM_007055.4:c.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₂=	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₉	dup(T)₁₂
GRCh38.p14 chr 10	NC_000010.11:g.78030500_78030521=	NC_000010.11:g.78030510_78030521del	NC_000010.11:g.78030511_78030521del	NC_000010.11:g.78030512_78030521del	NC_000010.11:g.78030513_78030521del	NC_000010.11:g.78030514_78030521del	NC_000010.11:g.78030515_78030521del	NC_000010.11:g.78030516_78030521del	NC_000010.11:g.78030517_78030521del	NC_000010.11:g.78030518_78030521del	NC_000010.11:g.78030519_78030521del	NC_000010.11:g.78030520_78030521del	NC_000010.11:g.78030521del	NC_000010.11:g.78030521dup	NC_000010.11:g.78030520_78030521dup	NC_000010.11:g.78030519_78030521dup	NC_000010.11:g.78030518_78030521dup	NC_000010.11:g.78030517_78030521dup	NC_000010.11:g.78030516_78030521dup	NC_000010.11:g.78030513_78030521dup	NC_000010.11:g.78030510_78030521dup
GRCh37.p13 chr 10	NC_000010.10:g.79790258_79790279=	NC_000010.10:g.79790268_79790279del	NC_000010.10:g.79790269_79790279del	NC_000010.10:g.79790270_79790279del	NC_000010.10:g.79790271_79790279del	NC_000010.10:g.79790272_79790279del	NC_000010.10:g.79790273_79790279del	NC_000010.10:g.79790274_79790279del	NC_000010.10:g.79790275_79790279del	NC_000010.10:g.79790276_79790279del	NC_000010.10:g.79790277_79790279del	NC_000010.10:g.79790278_79790279del	NC_000010.10:g.79790279del	NC_000010.10:g.79790279dup	NC_000010.10:g.79790278_79790279dup	NC_000010.10:g.79790277_79790279dup	NC_000010.10:g.79790276_79790279dup	NC_000010.10:g.79790275_79790279dup	NC_000010.10:g.79790274_79790279dup	NC_000010.10:g.79790271_79790279dup	NC_000010.10:g.79790268_79790279dup
POLR3A RefSeqGene	NG_029648.1:g.4020_4041=	NG_029648.1:g.4030_4041del	NG_029648.1:g.4031_4041del	NG_029648.1:g.4032_4041del	NG_029648.1:g.4033_4041del	NG_029648.1:g.4034_4041del	NG_029648.1:g.4035_4041del	NG_029648.1:g.4036_4041del	NG_029648.1:g.4037_4041del	NG_029648.1:g.4038_4041del	NG_029648.1:g.4039_4041del	NG_029648.1:g.4040_4041del	NG_029648.1:g.4041del	NG_029648.1:g.4041dup	NG_029648.1:g.4040_4041dup	NG_029648.1:g.4039_4041dup	NG_029648.1:g.4038_4041dup	NG_029648.1:g.4037_4041dup	NG_029648.1:g.4036_4041dup	NG_029648.1:g.4033_4041dup	NG_029648.1:g.4030_4041dup
RPS24 RefSeqGene (LRG_1145)	NG_012633.1:g.1741_1762=	NG_012633.1:g.1751_1762del	NG_012633.1:g.1752_1762del	NG_012633.1:g.1753_1762del	NG_012633.1:g.1754_1762del	NG_012633.1:g.1755_1762del	NG_012633.1:g.1756_1762del	NG_012633.1:g.1757_1762del	NG_012633.1:g.1758_1762del	NG_012633.1:g.1759_1762del	NG_012633.1:g.1760_1762del	NG_012633.1:g.1761_1762del	NG_012633.1:g.1762del	NG_012633.1:g.1762dup	NG_012633.1:g.1761_1762dup	NG_012633.1:g.1760_1762dup	NG_012633.1:g.1759_1762dup	NG_012633.1:g.1758_1762dup	NG_012633.1:g.1757_1762dup	NG_012633.1:g.1754_1762dup	NG_012633.1:g.1751_1762dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

33 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA	ss3832216214	Apr 26, 2020 (154)
2	KOGIC	ss3968229007	Apr 26, 2020 (154)
3	KOGIC	ss3968229008	Apr 26, 2020 (154)
4	KOGIC	ss3968229009	Apr 26, 2020 (154)
5	KOGIC	ss3968229010	Apr 26, 2020 (154)
6	GNOMAD	ss4221617396	Apr 26, 2021 (155)
7	GNOMAD	ss4221617397	Apr 26, 2021 (155)
8	GNOMAD	ss4221617398	Apr 26, 2021 (155)
9	GNOMAD	ss4221617399	Apr 26, 2021 (155)
10	GNOMAD	ss4221617400	Apr 26, 2021 (155)
11	GNOMAD	ss4221617401	Apr 26, 2021 (155)
12	GNOMAD	ss4221617402	Apr 26, 2021 (155)
13	GNOMAD	ss4221617403	Apr 26, 2021 (155)
14	GNOMAD	ss4221617405	Apr 26, 2021 (155)
15	GNOMAD	ss4221617406	Apr 26, 2021 (155)
16	GNOMAD	ss4221617407	Apr 26, 2021 (155)
17	GNOMAD	ss4221617408	Apr 26, 2021 (155)
18	GNOMAD	ss4221617409	Apr 26, 2021 (155)
19	GNOMAD	ss4221617410	Apr 26, 2021 (155)
20	GNOMAD	ss4221617411	Apr 26, 2021 (155)
21	GNOMAD	ss4221617412	Apr 26, 2021 (155)
22	GNOMAD	ss4221617413	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5198437926	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5198437927	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5198437928	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5198437929	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5284677864	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5284677865	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5480189792	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5744504493	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5744504494	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5744504495	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5744504496	Oct 16, 2022 (156)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 357357664 (NC_000010.11:78030499::T 4200/35222) Row 357357665 (NC_000010.11:78030499::TT 659/35090) Row 357357666 (NC_000010.11:78030499::TTT 29/35070)...	-	Apr 26, 2021 (155)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 24607008 (NC_000010.11:78030501:TT: 172/1702) Row 24607009 (NC_000010.11:78030503::T 58/1702) Row 24607010 (NC_000010.11:78030502:T: 39/1702)...	-	Apr 26, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 24607008 (NC_000010.11:78030501:TT: 172/1702) Row 24607009 (NC_000010.11:78030503::T 58/1702) Row 24607010 (NC_000010.11:78030502:T: 39/1702)...	-	Apr 26, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 24607008 (NC_000010.11:78030501:TT: 172/1702) Row 24607009 (NC_000010.11:78030503::T 58/1702) Row 24607010 (NC_000010.11:78030502:T: 39/1702)...	-	Apr 26, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 24607008 (NC_000010.11:78030501:TT: 172/1702) Row 24607009 (NC_000010.11:78030503::T 58/1702) Row 24607010 (NC_000010.11:78030502:T: 39/1702)...	-	Apr 26, 2020 (154)
56	8.3KJPN Submission ignored due to conflicting rows: Row 56407233 (NC_000010.10:79790257:TT: 1150/15850) Row 56407234 (NC_000010.10:79790257::T 292/15850) Row 56407235 (NC_000010.10:79790257:T: 49/15850)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 56407233 (NC_000010.10:79790257:TT: 1150/15850) Row 56407234 (NC_000010.10:79790257::T 292/15850) Row 56407235 (NC_000010.10:79790257:T: 49/15850)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 56407233 (NC_000010.10:79790257:TT: 1150/15850) Row 56407234 (NC_000010.10:79790257::T 292/15850) Row 56407235 (NC_000010.10:79790257:T: 49/15850)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 56407233 (NC_000010.10:79790257:TT: 1150/15850) Row 56407234 (NC_000010.10:79790257::T 292/15850) Row 56407235 (NC_000010.10:79790257:T: 49/15850)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 78341597 (NC_000010.11:78030499:TT: 2284/24714) Row 78341598 (NC_000010.11:78030499::T 643/24714) Row 78341599 (NC_000010.11:78030499:T: 90/24714)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 78341597 (NC_000010.11:78030499:TT: 2284/24714) Row 78341598 (NC_000010.11:78030499::T 643/24714) Row 78341599 (NC_000010.11:78030499:T: 90/24714)...	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 78341597 (NC_000010.11:78030499:TT: 2284/24714) Row 78341598 (NC_000010.11:78030499::T 643/24714) Row 78341599 (NC_000010.11:78030499:T: 90/24714)...	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 78341597 (NC_000010.11:78030499:TT: 2284/24714) Row 78341598 (NC_000010.11:78030499::T 643/24714) Row 78341599 (NC_000010.11:78030499:T: 90/24714)...	-	Oct 16, 2022 (156)
64	ALFA	NC_000010.11 - 78030500	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4221617413	NC_000010.11:78030499:TTTTTTTTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4221617412	NC_000010.11:78030499:TTTTTTTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4221617411	NC_000010.11:78030499:TTTTTTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4221617410	NC_000010.11:78030499:TTTTTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4221617409	NC_000010.11:78030499:TTTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4221617408	NC_000010.11:78030499:TTTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4221617407	NC_000010.11:78030499:TTTTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4221617406	NC_000010.11:78030499:TTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3968229010	NC_000010.11:78030500:TTT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5198437926	NC_000010.10:79790257:TT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4221617405, ss5744504493	NC_000010.11:78030499:TT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3968229007	NC_000010.11:78030501:TT:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5198437928	NC_000010.10:79790257:T:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5284677864, ss5744504495	NC_000010.11:78030499:T:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3968229009	NC_000010.11:78030502:T:	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3832216214, ss5198437927	NC_000010.10:79790257::T	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617396, ss5480189792, ss5744504494	NC_000010.11:78030499::T	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3968229008	NC_000010.11:78030503::T	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5198437929	NC_000010.10:79790257::TT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617397, ss5284677865, ss5744504496	NC_000010.11:78030499::TT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617398	NC_000010.11:78030499::TTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12551361900	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617399	NC_000010.11:78030499::TTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617400	NC_000010.11:78030499::TTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617401	NC_000010.11:78030499::TTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617402	NC_000010.11:78030499::TTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4221617403	NC_000010.11:78030499::TTTTTTTTTTTT	NC_000010.11:78030499:TTTTTTTTTTTT… NC_000010.11:78030499:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1159327463

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1159327463